Canonical Allele Identifier: CA2195408414

Gene: VPS33B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022328G= , CM000677.2:g.91022328G=	GRCh38
NC_000015.9:g.91565558G= , CM000677.1:g.91565558G=	GRCh37
NC_000015.8:g.89366562G=	NCBI36
NG_012162.1:g.5276C= , LRG_884:g.5276C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-79C= MANE Select	ENSP00000327650.4:n.-79C=
ENST00000643536.1:c.-79C=	ENSP00000494429.1:n.-79C=
ENST00000333371.7:c.-79C=	ENSP00000327650.3:n.-79C=
ENST00000535906.1:c.-79C=	ENSP00000444053.1:n.-79C=
ENST00000556096.6:n.276C=
ENST00000557358.1:n.269C=
ENST00000574755.5:c.-79C=	ENSP00000460413.1:n.-79C=
NM_001289148.1:c.-79C=	NP_001276077.1:n.-79C=
NM_001289149.1:c.-290C=	NP_001276078.1:n.-290C=
NM_018668.4:c.-79C= , LRG_884t1:c.-79C=	NP_061138.3:n.-79C=
XM_005254884.2:c.-79C=	XP_005254941.1:n.-79C=
XM_005254887.1:c.-209C=	XP_005254944.1:n.-209C=
XM_005254888.2:c.-79C=	XP_005254945.1:n.-79C=
XM_011521448.1:c.-392C=	XP_011519750.1:n.-392C=
XM_017022075.2:c.-440C=	XP_016877564.1:n.-440C=
XM_017022076.1:c.-297C=	XP_016877565.1:n.-297C=
XR_001751213.2:n.258C=
NM_018668.5:c.-79C= MANE Select	NP_061138.3:n.-79C=